ClinVar Miner

Submissions for variant NM_000057.4(BLM):c.1563A>G (p.Pro521=)

gnomAD frequency: 0.00003  dbSNP: rs763118109
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001492293 SCV001696902 likely benign Bloom syndrome 2023-11-01 criteria provided, single submitter clinical testing
Ambry Genetics RCV002405158 SCV002708738 likely benign Hereditary cancer-predisposing syndrome 2017-03-20 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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